Description
QAV SpecialistA global Biopharmaceutical leader is currently looking for a QAV Specialist to join their team on a new build project based in Ireland.
The responsibilities of the QAV Specialist will include:
- Provide quality and cGMP input and oversight for all start-up project activities through commercial readiness and ongoing product disposition.
- Provide QA support for risk based verification activities in the capacity of Quality Assurance Subject Matter Expert. Review and approval equipment/utilities verification documentation from design to post execution.
- Participate in verification quality risk assessments and provide quality oversight to ensure verification quality risk assessments are effectively maintained/controlled.
The successful QAV Specialist will possess the below experience:
- Min 5 years QA experience in a pharmaceutical manufacture/biopharmaceutical environment. (BDS experience is essential).
- Must have strong process knowledge to include upstream and/or downstream processing.
- An ability to work independently, as well as a member of a team in a dynamic, fast-paced environment.
- Excellent communication & presentation skills are essential.
If you are interested in becoming a QAV Specialist, please apply.